Synthesis and trypanocidal activity of ent-kaurane glycosides.

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MetadadosDescriçãoIdioma
Autor(es): dc.creatorBatista, Ronan-
Autor(es): dc.creatorHumberto, Jorge Luiz-
Autor(es): dc.creatorChiari, Egler-
Autor(es): dc.creatorOliveira, Alaíde Braga de-
Data de aceite: dc.date.accessioned2019-11-06T13:33:31Z-
Data de disponibilização: dc.date.available2019-11-06T13:33:31Z-
Data de envio: dc.date.issued2015-04-14-
Data de envio: dc.date.issued2015-04-14-
Data de envio: dc.date.issued2007-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/handle/123456789/5089-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/558052-
Descrição: dc.descriptionNovel ent-kaurane glucosides were synthezised by a Koenigs–Knorr reaction between C17 and C19 alcohols derived from kaurenoic acid and 2,3,4,6-tetra-O-acetyl-glucopyranosyl bromide, followed by the hydrolysis of the acetates. Main products were assayed in vitro and in vivo against blood trypomastigote forms of Trypanosoma cruzi, the aetiological agent of Chagas’ disease (American trypanosomiasis). The results allowed to establish structure–activity relationships among these derivatives, as well as pointed out the C19-methylester-C17-O-glucoside as a potential trypanocidal agent, whose trypanocidal profile was shown to be comparable to those of gentian violet and benznidazole.-
Idioma: dc.languageen-
Direitos: dc.rightsO Periódico Bioorganic & Medicinal Chemistry concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3581340483210.-
Palavras-chave: dc.subjectKaurenoic acid-
Palavras-chave: dc.subjectKoenigs–Knorr reaction-
Palavras-chave: dc.subjectTrypanosoma cruzi-
Título: dc.titleSynthesis and trypanocidal activity of ent-kaurane glycosides.-
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